drugset / Trial / NCT01960855

A Study Investigating the Efficacy and Safety of ABT-494 Given With Methotrexate in Subjects With Rheumatoid Arthritis Who Failed Anti-Tumor Necrosis Factor (TNF) Biologic Therapy

NCT01960855 ↗

Phase 2 Completed 276 enrolled AbbVie
RandomizedParallel-groupQuadruple-blindTreatment

Summary

The primary objective is to compare the safety and efficacy of multiple doses of ABT-494 versus placebo in moderately to severely active RA subjects on stable background MTX therapy with inadequate response or intolerance to anti-TNF biologic therapy.

Timeline

Start
2013-10
Primary completion
2015-07
Completion
2015-07

Outcome

Met primary endpoint

release “BALANCE-I and BALANCE-II achieved ACR20 at week 12 across all dose levels, except the lowest dose in BALANCE-II.” abbvie.com ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Upadacitinib Small molecule 3 mg Oral
Subject Upadacitinib Small molecule 6 mg Oral
Subject Upadacitinib Small molecule 12 mg Oral
Subject Upadacitinib Small molecule 18 mg Oral

Indications